Shin Lin

28.3k total citations · 2 hit papers
38 papers, 4.1k citations indexed

About

Shin Lin is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Shin Lin has authored 38 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Surgery and 9 papers in Genetics. Recurrent topics in Shin Lin's work include Cardiac Structural Anomalies and Repair (6 papers), Genetic Associations and Epidemiology (5 papers) and Mechanical Circulatory Support Devices (5 papers). Shin Lin is often cited by papers focused on Cardiac Structural Anomalies and Repair (6 papers), Genetic Associations and Epidemiology (5 papers) and Mechanical Circulatory Support Devices (5 papers). Shin Lin collaborates with scholars based in United States, Austria and United Kingdom. Shin Lin's co-authors include David J. Cutler, Yiing Lin, Samuel Yang, Aravinda Chakravarti, Aravinda Chakravarti, Bing Ren, Inkyung Jung, Anthony D. Schmitt, Charlotte A. Gaydos and Seungkyung Park and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Shin Lin

37 papers receiving 4.0k citations

Hit Papers

A Compendium of Chromatin Contact Maps Reveals Spatially ... 2015 2026 2018 2022 2016 2015 100 200 300 400

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Shin Lin United States 26 2.1k 1.3k 536 400 322 38 4.1k
Peter Williamson Australia 29 1.2k 0.6× 460 0.4× 283 0.5× 202 0.5× 576 1.8× 142 5.0k
Yuko Wada Japan 31 2.3k 1.1× 313 0.2× 895 1.7× 339 0.8× 119 0.4× 249 4.8k
Raju Kucherlapati United States 39 4.4k 2.1× 2.1k 1.6× 231 0.4× 108 0.3× 224 0.7× 70 6.9k
Emmanuel Dias‐Neto Brazil 38 1.6k 0.8× 653 0.5× 270 0.5× 103 0.3× 64 0.2× 129 4.2k
Eleanor Feingold United States 38 2.2k 1.0× 2.3k 1.8× 423 0.8× 79 0.2× 78 0.2× 185 5.6k
Steven L. Stice United States 47 5.4k 2.5× 2.3k 1.7× 802 1.5× 812 2.0× 65 0.2× 176 7.7k
Karen J. Taylor United Kingdom 34 1.3k 0.6× 532 0.4× 631 1.2× 199 0.5× 501 1.6× 105 3.9k
Jing Zhou United States 37 2.0k 1.0× 575 0.4× 133 0.2× 161 0.4× 302 0.9× 98 4.5k
Xiaolin Wu United States 47 5.1k 2.4× 2.1k 1.6× 196 0.4× 135 0.3× 193 0.6× 172 8.5k
Felipe Moreno Spain 46 4.2k 2.0× 1.7k 1.3× 299 0.6× 87 0.2× 331 1.0× 131 6.3k

Countries citing papers authored by Shin Lin

Since Specialization
Citations

This map shows the geographic impact of Shin Lin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Shin Lin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shin Lin more than expected).

Fields of papers citing papers by Shin Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shin Lin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Shin Lin. The network helps show where Shin Lin may publish in the future.

Co-authorship network of co-authors of Shin Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Shin Lin. A scholar is included among the top collaborators of Shin Lin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Shin Lin. Shin Lin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Lin, Shin, Ioannis Dimarakis, Elina Minami, et al.. (2024). Highly sensitized patients listed for heart after liver transplantation with or without domino. The Journal of Heart and Lung Transplantation. 44(1). 125–128. 2 indexed citations
2.
Read, David F., Gregory T. Booth, Riza M. Daza, et al.. (2024). Single-cell analysis of chromatin and expression reveals age- and sex-associated alterations in the human heart. Communications Biology. 7(1). 1052–1052. 5 indexed citations
3.
Dimarakis, Ioannis, Shin Lin, Aris Karatasakis, et al.. (2024). Pilot Experience with Heart After Liver Transplantation with Domino (HALT-D) for Highly Allosensitized Recipients: Midterm Outcomes. The Journal of Heart and Lung Transplantation. 43(4). S495–S495.
4.
Fu, Xiaonan, Li Sun, Runze Dong, et al.. (2022). Polony gels enable amplifiable DNA stamping and spatial transcriptomics of chronic pain. Cell. 185(24). 4621–4633.e17. 80 indexed citations
5.
Friedman, Clayton E., et al.. (2022). Generation of human iPSC line from an arrhythmogenic cardiomyopathy patient with a DSP protein-truncating variant. Stem Cell Research. 66. 102987–102987. 6 indexed citations
6.
Kim, Daniel Seung, Viviana I. Risca, David L. Reynolds, et al.. (2021). The dynamic, combinatorial cis-regulatory lexicon of epidermal differentiation. Nature Genetics. 53(11). 1564–1576. 42 indexed citations
7.
Li, Song, Jennifer A. Beckman, Richard K. Cheng, et al.. (2020). Accuracy of Doppler Blood Pressure Measurement in Heart Mate 3 Ventricular Assist Device Patients. ESC Heart Failure. 7(6). 4241–4246. 5 indexed citations
8.
Xiao, Zhenyu, Haniee Chung, Babak Banan, et al.. (2015). Antibody mediated therapy targeting CD47 inhibits tumor progression of hepatocellular carcinoma. Cancer Letters. 360(2). 302–309. 143 indexed citations
9.
Lin, Yiing, Shin Lin, Susan Kennedy, et al.. (2015). Novel APC promoter and exon 1B deletion and allelic silencing in three mutation-negative classic familial adenomatous polyposis families. Genome Medicine. 7(1). 42–42. 20 indexed citations
10.
Fotiou, Elisavet, Silvia Martin‐Almedina, Michael A. Simpson, et al.. (2015). Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis. Nature Communications. 6(1). 8085–8085. 223 indexed citations
11.
Schultz, Matthew D., Yupeng He, John W. Whitaker, et al.. (2015). Human body epigenome maps reveal noncanonical DNA methylation variation. Nature. 523(7559). 212–216. 424 indexed citations breakdown →
12.
Yamada, Ryotaro, Ingela Schnittger, Jennifer A. Tremmel, et al.. (2012). Abstract 12745: Is Myocardial Bridging Truly Benign? Impact of Myocardial Bridging Induced Arterial Compression on Atherosclerotic Plaque Formation. Circulation. 126(2). 372–3. 1 indexed citations
14.
Lin, Yiing, Shin Lin, Mark Watson, et al.. (2009). A gene expression signature that predicts the therapeutic response of the basal-like breast cancer to neoadjuvant chemotherapy. Breast Cancer Research and Treatment. 123(3). 691–699. 22 indexed citations
15.
Lin, Shin, Benilton S. Carvalho, David J. Cutler, et al.. (2008). Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays. Genome Biology. 9(4). R63–R63. 25 indexed citations
16.
Marchini, Jonathan, David J. Cutler, Nick Patterson, et al.. (2006). A Comparison of Phasing Algorithms for Trios and Unrelated Individuals. The American Journal of Human Genetics. 78(3). 437–450. 231 indexed citations
17.
Lin, Shin, et al.. (2005). Phenotype Severity and Genetic Variation at the Disease Locus: An Investigation of Nail Dysplasia in the Nail Patella Syndrome. Annals of Human Genetics. 69(1). 1–8. 41 indexed citations
18.
Emison, E, Andrew S. McCallion, Carl Kashuk, et al.. (2005). A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk. Nature. 434(7035). 857–863. 337 indexed citations
19.
Lin, Shin, Aravinda Chakravarti, & David J. Cutler. (2004). Haplotype and Missing Data Inference in Nuclear Families. Genome Research. 14(8). 1624–1632. 36 indexed citations
20.
Lin, Shin, Aravinda Chakravarti, & David J. Cutler. (2004). Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies. Nature Genetics. 36(11). 1181–1188. 109 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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